A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1142119



Internal ID19286003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:102299022..102303476hg38UCSC Ensembl
Outerchr11:102169753..102174207hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg384455
hg194455
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3983710, nssv3988023
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1142119
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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